scholarly journals Formation Procedure of Reaction Phases in Al Hot Dipping Process of Steel

Metals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 820 ◽  
Author(s):  
Dongik Shin ◽  
Jeong-Yong Lee ◽  
Hoejun Heo ◽  
Chung-Yun Kang

This study investigated the nucleation and growth mechanism of reaction layers and phases of hot-dipped boron steel in pure Al at 690 °C for 0–120 s. In the case of a dipping time of 30 s, reaction nuclei of width 10–15 μm and height 10 μm were formed on the steel surface in the flow direction of the liquid Al. This reaction layer was formed as a mixture of θ (Fe4Al13) phase of several nm to 2 μm, θ and η (Fe2Al5) of several nm, a columnar η region, and a β (FeAl) region of 500 nm thickness at the steel interface. At the grain boundaries of ferrite, in contact with the η phase, κ (Fe3AlC) was formed. Using the calculated Fe-Al phase diagram, it was determined that when Fe was dissolved in liquid Al from the steel above 2.5 at% (0.6 wt%), the θ phase was formed. Although most of the θ phases continuously grew toward the liquid phase, the θ phase in contact with the steel was transformed into the η phase with minimal differences in composition due to the inter-diffusion of Al and Fe. It was therefore concluded that the η phase formed at the interface became a growth nucleus and grew in a columnar form toward the steel.

1989 ◽  
Vol 4 (4) ◽  
pp. 795-801 ◽  
Author(s):  
C. J. Jou ◽  
J. Washburn

A nucleation-and-growth mechanism for the twin formation in YBa2Cu3O7–δ superconductors based on the oxygen uptake rate curve and published transmission electron microscopic observations is proposed together with an oxygen-depleted twin boundary model. The difficulty of reaching stoichiometric YBa2Cu3O7 is explained.


2021 ◽  
Vol 12 (5) ◽  
pp. 6776-6787

A Co-doped ZnO layer was prepared by electrodeposition method on indium doped tin oxide (ITO) substrate using a cathodic reduction from nitrate medium with different doping percentages of cobalt. The bath temperature was controlled at 70 °C. The films were cathodically electrodeposited in a bath containing 5 mM Zn(NO3)2. 6H2O, while the source of Co is Co(NO3)2.6H2O where 0.1M KNO3 was used as supporting electrolyte. The nucleation and growth mechanism of Co-doped ZnO nuclei have been studied by cyclic voltammetry and chronoamperometry. The cyclic voltammetry shows that the electrodeposition of ZnO and Co-doped ZnO at a negative potential around -1.0 V versus saturated calomel electrode (SCE) is a quasi-reversible reaction controlled by the diffusion process. Comparing current transients curves obtained by the chronoamperometric method with the theoretical curves of current density j versus t ½ allows us to say that the nucleation is 3D instantaneous, as shown in SEM analysis. The presence of Co does not modify the nucleation and growth mechanism. The XRD patterns show that the substitution of zinc by cobalt does not change the würtzite crystal structure, but the crystallite size decreases with the cobalt percentage. The transmittance spectra indicate that the Co-doped ZnO films are transparent in the visible range. The optical gap increases with the doping percentage of cobalt.


2012 ◽  
Vol 134 (9) ◽  
pp. 4384-4392 ◽  
Author(s):  
Galyna Krylova ◽  
Lisandro J. Giovanetti ◽  
Felix G. Requejo ◽  
Nada M. Dimitrijevic ◽  
Alesia Prakapenka ◽  
...  

Coatings ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 467 ◽  
Author(s):  
Dongik Shin ◽  
Jeong-Yong Lee ◽  
Hoejun Heo ◽  
Chung-Yun Kang

Microstructural evolution and formation mechanism of reaction layer for 22MnB5 steel hot-dipped in Al–10Si (in wt %) alloy was investigated. The microstructural identification of the reaction layer was characterized via transmission electron microscopy and electron backscatter diffraction. In addition, the formation mechanisms of the phases were discussed with vertical section (isopleth) of the (Al–Si–Fe) ternary system. The solidified Al–Si coating layer consisted of three phases of Al, Si, and τ5 (Al8Fe2Si). The reaction layer on the Al–Si coating layer side is a fine τ5 phase (Al8Fe2Si) of 5 μm thickness. The layer on the steel side consisted of an η phase (Fe2Al5) of thickness of 500 nm or less. τ1 (Al2Fe3Si3, triclinic) phase of 200-nm-thickness was formed in the η phase, and κ phase (Fe3AlC) of 40–50 nm thickness was formed between η phase and steel. The τ5 phase was formed by isothermal solidification at 690 °C in the liquid Al–10 wt % Si when 3.73–29.0 wt % of Fe was dissolved from the boron steel into the Al–Si liquid bath. It was considered that the η phase was formed by the diffusion reaction of Al, Si, and Fe between τ5 and ferrite steel. κ (Fe3AlC) phase was formed by the reaction of the carbon, which is barely employed in η and τ phases, and diffused Al.


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